Published August 2013 | Version v1
Journal article

Water-soluble CdSe/CdS and CdSe/CdxZn1−xS quantum dots with tunable and narrow luminescent spectra and high photoluminescence efficiency

  • 1. University of Jinan, Shandong Provincial Key Laboratory of Preparation and Measurement of Building Materials, Key Laboratory of Inorganic Functional Materials of Shandong Universities, School of Material Science and Engineering (China)
  • 2. Shandong Polytechnic University, Key Laboratory of Processing and Testing Technology of Glass and Functional Ceramics of Shandong Province, Department of Materials Science and Engineering (China)

Description

Nearly monodisperse CdSe/CdS and CdSe/CdxZn1−xS core–shell quantum dots (QDs) were synthesized by the epitaxial growth of CdS or CdxZn1–xS shells on pre-synthesized CdSe cores through a facile organic route. The thickness effect of CdS and CdxZn1−xS shells on the properties of resulting core–shell QDs, such as the photoluminescence (PL) efficiency, PL full width at half-maximum (fwhm), and PL decay lifetime, were investigated. The PL efficiency is greatly enhanced from 9 % of CdSe cores to 64 % of CdSe/CdxZn1−xS core–shell QDs. The PL spectra are narrowed after coating (fwhm ∼28–32 nm). The alloy CdxZn1−xS shell is especially effective to enhance the PL efficiency, and it leads to a smaller red-shift in PL spectra compared with that of the CdS shell. The water-soluble CdSe/CdxZn1−xS core–shell QDs were obtained by the encapsulation of amphiphilic poly(styrene-co-maleic anhydride) (PSMA)–ethanolamine (EA) polymers, which was initially dispersed in oil phase. It was found that the CdSe/CdxZn1−xS QDs in water still retained a high PL efficiency as well as a small value in fwhm after encapsulating the CdSe/CdxZn1−xS QDs with PSMA–EA polymers, expanding the applications of these core–shell QDs in aqueous environment

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Identifiers

Publishing Information

Journal Title
Journal of Nanoparticle Research
Journal Volume
15
Journal Issue
8
Journal Page Range
p. 1-11
ISSN
1388-0764

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Copyright (c) 2013 Springer Science+Business Media Dordrecht